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FDA 510(k) Applications Submitted by TIM REEVES
FDA 510(k) Number
Submission Date
Device Name
Applicant
K032212
07/21/2003
KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A
KYPHON, INC.
K062038
07/19/2006
X-STEN MILD TOOL KIT, MODEL MTK-0001
X-STEN CORP.
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